850522P

Avanti

Facade^™-EM

Name: Facade<SUP>™</SUP>-EM
Brand: AVANTI
Price: 66200 HUF

Avanti Research^™ - A Croda Brand

Synonym(s):

FA-3; 3α-hydroxy-7α,12α-di-((O-Β-D-maltopyranosyl)ethyloxy)-cholane

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25 MG

HUF 66,200.00

1 G

HUF 826,000.00

HUF 66,200.00

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About This Item

Empirical Formula (Hill Notation):

C₅₂H₉₀O₂₅

CAS Number:

1429405-95-7

Molecular Weight:

1115.26

MDL number:

MFCD32697036

UNSPSC Code:

12161902

NACRES:

NA.25

Key Documents

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Product Name

Facade^™-EM, 3α-hydroxy-7α,12α-di-((O-β-D-maltosyl)-2-hydroxyethoxy)-cholane, powder

SMILES string

[H][C@@]12[C@]([C@](CC[C@@H](O)C3)(C)[C@]3([H])C[C@H]2OCCO[C@@H]4[C@@H](O)[C@H](O)[C@@H](O[C@H]5[C@@H](O)[C@H](O)[C@@H](O)[C@H](CO)O5)[C@H](CO)O4)([H])C[C@H](OCCO[C@H]6[C@H](O)[C@@H](O)[C@H](O[C@@H]7[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O7)[C@@H](CO)O6)[C@@]

assay

>99% (TLC)

form

powder

mol wt

1115.26 g/mol

packaging

pkg of 1 × 1 g (850522P-1g)
pkg of 1 × 200 mg (850522P-200mg)
pkg of 1 × 25 mg (850522P-25mg)

manufacturer/tradename

Avanti Research^™ - A Croda Brand 850522P

shipped in

dry ice

storage temp.

−20°C

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1 of 4

This Item	850537P	850562P	C6445
Avanti 850522P Facade^™-EM	Avanti 850537P Facade^™-TEM	Avanti 850562P Facade^™ Detergent Kit	Sigma-Aldrich C6445 Sodium cholate hydrate
form powder	form powder	form powder	form powder
assay >99% (TLC)	assay >99% (TLC)	assay 99% (TLC)	assay ≥99%
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. -
mol wt 1115.26 g/mol	mol wt 1483.59 g/mol	mol wt -	mol wt micellar avg mol wt 900-1300
packaging pkg of 1 × 1 g (850522P-1g)	packaging pkg of 1 × 25 mg (850537P-25mg)	packaging -	packaging -
manufacturer/tradename Avanti Research^™ - A Croda Brand 850522P	manufacturer/tradename Avanti Research^™ - A Croda Brand 850537P	manufacturer/tradename Avanti Research^™ - A Croda Brand	manufacturer/tradename -

Application

Facade^™EM (3α-hydroxy-7α,12α-di-((O-β-D-maltosyl)-2-hydroxyethoxy)-cholane) may be used:

as a facial amphiphile detergent to purify protoxin-II (ProTx2)-voltage-sensor domain II (VSD2)-voltage-gated sodium (NavAb) channel[1]
as an additive in fluorescence quenching experiments of pentaene-SM 18[2]
to form isotropic bicelles with p75 for nuclear magnetic resonance (NMR) studies[3]

Biochem/physiol Actions

Facades can be used for the crystallization of membrane proteins since they are considered as optimized membrane mimetics.[3]

General description

Facade-EM is a two-dimensional amphiphile with hydrophobic and hydrophilic faces that has superior ability to stabilize integral membrane proteins. This new class of detergents represents a departure from traditional one-dimensional polar-head/nonpolar-tail molecules.

Packaging

20 mL Clear Glass Screw Cap Vial (850522P-1g)

20 mL Clear Glass Screw Cap Vial (850522P-200mg)

5 mL Amber Glass Screw Cap Vial (850522P-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Facade is a trademark of Avanti Polar Lipids, LLC

Storage Class

11 - Combustible Solids

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Certificates of Analysis (COA)

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Mutual recognition of sphingolipid molecular species in membranes.

Andreas Max Ernst et al.

Biochimica et biophysica acta, 1818(11), 2616-2622 (2012-06-16)

In membranes liquid disordered (l(d)) and liquid ordered (l(o)) domains can exist that differ in fluidity and function. L(o) areas are predominantly composed of cholesterol and sphingomyelin (SM). Study of the formation of such domains is hampered by a lack

Structural Basis of Nav1.7 Inhibition by a Gating-Modifier Spider Toxin.

Hui Xu et al.

Cell, 176(4), 702-715 (2019-01-22)

Voltage-gated sodium (Nav) channels are targets of disease mutations, toxins, and therapeutic drugs. Despite recent advances, the structural basis of voltage sensing, electromechanical coupling, and toxin modulation remains ill-defined. Protoxin-II (ProTx2) from the Peruvian green velvet tarantula is an inhibitor

Faccade detergents as bicelle rim-forming agents for solution NMR spectroscopy

Mineev KS, et al.

Nanotech. in Catalysis, 6(1), 93-103 null

Designing facial amphiphiles for the stabilization of integral membrane proteins.

Qinghai Zhang et al.

Angewandte Chemie (International ed. in English), 46(37), 7023-7025 (2007-08-11)

Steroid-based facial amphiphiles for stabilization and crystallization of membrane proteins.

Sung Chang Lee et al.

Proceedings of the National Academy of Sciences of the United States of America, 110(13), E1203-E1211 (2013-03-13)

Amphiphile selection is a critical step for structural studies of membrane proteins (MPs). We have developed a family of steroid-based facial amphiphiles (FAs) that are structurally distinct from conventional detergents and previously developed FAs. The unique FAs stabilize MPs and

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Facade^™-EM